Evaluation model for rat neurotoxicity of parotitis virus
A mumps virus and neurovirulence technology, applied in the direction of instruments, biological systems, analytical materials, etc., can solve problems such as unsatisfactory, time-consuming slice processing, complicated operation, etc.
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[0067] Example 1: Establishment of a rat model for evaluation of mumps virus neurovirulence
[0068] 1.1 Animal and virus dilution
[0069] Four pregnant Wistar rats of SPF grade were selected and randomly divided into four groups, namely A, B, C and D (the number of suckling rats in each group was not less than 10). Among them, group A was inoculated with DMEM medium as the control group, group B was inoculated with the vaccine strain, group C was inoculated with wild mumps strain passaged by Vero cells for 10 times, and group D was inoculated with wild mumps strain. B, C, D 3 groups are 4.0lg CCID with DMEM culture medium dilution virus titer 50 / mL.
[0070] 1.2 Virus inoculation
[0071] After the birth of the mother mouse, fix the 1-day-old suckling mouse, draw 10 μL of the virus liquid with a sterilized 20 μL micro-syringe (specification 27G), and inject it at the middle of the anterior blotch and herringbone point of the brain of the suckling mouse, on the left side ...
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